Maarten P van den Berg
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Explore the profile of Maarten P van den Berg including associated specialties, affiliations and a list of published articles.
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206
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5457
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Recent Articles
1.
Krijger Juarez C, Proost V, Tanck M, Dittmann S, Bos J, Crotti L, et al.
Heart Rhythm
. 2024 Dec;
PMID: 39675651
Background: Congenital long QT syndrome (LQTS) is characterized by delayed ventricular repolarization, predisposing to potentially lethal ventricular arrhythmias. The variability in disease severity among patients remains largely unexplored, underscoring the...
2.
Accord R, Koster C, Dulfer E, du Marchie Sarvaas G, Maass S, Berger R, et al.
Eur J Pediatr
. 2024 Nov;
184(1):25.
PMID: 39557716
The purpose of this study is to evaluate the diagnostic and therapeutic yield of a specialized clinic for children with suspicion of a hereditary thoracic aortic disease (HTAD), including Marfan...
3.
van de Leur R, de Brouwer R, Bleijendaal H, Verstraelen T, Mahmoud B, Perez-Matos A, et al.
Heart Rhythm
. 2024 Feb;
21(7):1102-1112.
PMID: 38403235
Background: Phospholamban (PLN) p.(Arg14del) variant carriers are at risk for development of malignant ventricular arrhythmia (MVA). Accurate risk stratification allows timely implantation of intracardiac defibrillators and is currently performed with...
4.
Accord R, Mecozzi G, Aalberts J, Nijs J, Ter Weeme M, van Aarnhem E, et al.
Interdiscip Cardiovasc Thorac Surg
. 2023 Dec;
37(6).
PMID: 38109664
Objectives: The most recent valve-sparing root replacement technique combines the advantages of the reimplantation (David) and remodelling (Yacoub) techniques. The aortic root is reconstructed according to the remodelling technique, the...
5.
Taha K, van de Leur R, Vessies M, Mast T, Cramer M, Cauwenberghs N, et al.
Int J Cardiovasc Imaging
. 2023 Aug;
39(11):2149-2161.
PMID: 37566298
Echocardiographic deformation curves provide detailed information on myocardial function. Deep neural networks (DNNs) may enable automated detection of disease features in deformation curves, and improve the clinical assessment of these...
6.
Proost V, van den Berg M, Remme C, Wilde A
Neth Heart J
. 2023 Jul;
31(7-8):263-271.
PMID: 37474841
The SCN5A-1795insD founder variant is a unique SCN5A gene variant found in a large Dutch pedigree that first came to attention in the late 1950s. To date, this is still...
7.
van Lint F, Hassanzada F, Verstraelen T, Wang W, Bosman L, van der Zwaag P, et al.
Neth Heart J
. 2023 Jul;
31(7-8):291-299.
PMID: 37474840
Background: Endurance and frequent exercise are associated with earlier onset of arrhythmogenic right ventricular cardiomyopathy (ARVC) and ventricular arrhythmias (VA) in desmosomal gene variant carriers. Individuals with the pathogenic c.40_42del;...
8.
Nagyova E, Hoorntje E, Te Rijdt W, Bosman L, Syrris P, Protonotarios A, et al.
J Cardiovasc Transl Res
. 2023 Jul;
16(6):1276-1286.
PMID: 37418234
The presence of multiple pathogenic variants in desmosomal genes (DSC2, DSG2, DSP, JUP, and PKP2) in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) has been linked to a severe phenotype....
9.
de Brouwer R, Te Rijdt W, Hoorntje E, Amin A, Asselbergs F, Cox M, et al.
Eur Heart J
. 2023 May;
44(40):4284-4287.
PMID: 37210081
No abstract available.
10.
Hoorntje E, Burns C, Marsili L, Corden B, Parikh V, Meerman G, et al.
Circ Genom Precis Med
. 2022 Dec;
16(1):e003672.
PMID: 36580316
Background: Truncating variants in desmoplakin (tv) are an important cause of arrhythmogenic cardiomyopathy; however the genetic architecture and genotype-specific risk factors are incompletely understood. We evaluated phenotype, risk factors for...